Yang Shangwen,Shao Mingran,Yang Xianfeng,Hu Anning,Wang Zhong,Jiang Hui,Zhu Bin,Zhang Bing,Xin Xiaoyan.A feasibility study on “Tri-Low” technology in combination with iterative model reconstruction(IMR) algorithm in CT angiography(CTA) of the head-and-neck vessels[J].Chinese Journal of Radiological Medicine and Protection,2017,37(1):62-67
A feasibility study on “Tri-Low” technology in combination with iterative model reconstruction(IMR) algorithm in CT angiography(CTA) of the head-and-neck vessels
Received:August 04, 2016  
DOI:10.3760/cma.j.issn.0254-5098.2017.01.012
KeyWords:Angiography  Tomography, X-ray computed  Radiation dose  Iterative reconstruction
FundProject:江苏省卫生厅青年科研课题(Q201410)
Author NameAffiliation
Yang Shangwen Deparment of Radiology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, 210008, China 
Shao Mingran Deparment of Radiology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, 210008, China 
Yang Xianfeng Deparment of Radiology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, 210008, China 
Hu Anning Deparment of Radiology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, 210008, China 
Wang Zhong Deparment of Radiology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, 210008, China 
Jiang Hui Deparment of Radiology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, 210008, China 
Zhu Bin Deparment of Radiology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, 210008, China 
Zhang Bing Deparment of Radiology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, 210008, China 
Xin Xiaoyan Deparment of Radiology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, 210008, China 
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Abstract::
      Objective To evaluate the feasibility of low-tube-voltage,low injection rate,low contrast agent dosage in combination with iterative model reconstruction(IMR) algorithm in CT angiography(CTA) of the head-and-neck vessels.Methods Sixty patients who underwent CT angiography of the head-and-neck vessels were randomly divided into groups A and B with 30 cases in each group. Patients in group A received a conventional scan with 120 kVp and filterback projected(FBP) reconstruction. Patients in group B received a low-dose scan with 80 kVp, and image reconstruction with FBP(group B1) and IMR(group B2) algorithm. The contrast agent protocol were as follows:the injection time in all patients was 10s, the injection rate was 4.5-5.5 ml/s in group A while 3.5-4.0 ml/s in group B. The CT values of artery, image noise, signal to noise ratio(SNR) and contrast to noise ratio(CNR) were measured and compared among three groups with One-way ANOVA analysis. Image quality was evaluated by two radiologists with five scale method, and compared with Kruskal-Wallis test. The CT dose index volume (CTDIvol) and dose length product (DLP) were recorded and compared between groups with two independent samples t-test. Results The image quality scores of groups A, B1and B2 were 3-5, 2-4 and 3-5, respectively.Image quality of twelve patients in group B1 couldn't meet the diagnostic requirements but none in group A and B2.The objective image parameters SNR and CNR for group B2 were equal to group A(P>0.05), while those for group B1 were lower than group A(t=13.39, 9.45,P<0.05) and group B2(t=-12.14, -9.96, P<0.05). CTDIvol and DLP for group B were separately 80.9%, 81.3% lower than those of group A(t=39.1, 32.2, P<0.05). The injection rate and contrast agent volume for group B were separately 22.0%, 22.1% lower than those of group A(t=20.8, 20.8, P<0.01).Conclusions It is feasible in CT angiography of the head-and-neck vessels with lower tube-voltage, lower injection rate, lower contrast agent dose and combining with iterative model reconstruction algorithm. This protocol can reduce the radiation dose by 81.3% while maintaining image quality.Trial registration Chinese clinical trial registry,ChiCTR-BOC-16010060.
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